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Mixture of Liposomal Bupivacaine and Bupivacaine for TAP Block for Open Hysterectomy

Hysterectomy Clinical Trial

Official title:
Mixture of Liposomal Bupivicaine and Bupivicaine Hydrogen Chloride (HCl) May Provide Faster and Longer Lasting Analgesia in Transversus Abdominis Block for Patient Having Open Abdominal Hysterectomies

Clinical Trial Summary

The goal of this study is to evaluate the effectiveness of different formulations of bupivacaine infiltrated into the transversus abdominis plane (TAP) on post-operative pain management after open abdominal hysterectomy.

Clinical Trial Description

All eligible patients who consent to the study will be randomized to one of three groups. Group 1 will receive a TAP block with 60 mL 0.25% bupivacaine. Group 2 will receive a TAP block with 20 mL liposomal bupivacaine and 40 mL saline. Group 3 will receive a TAP block with 20 mL liposomal bupivacaine and 40 mL 0.25% bupivacaine. Patients will be assessed in the post-anesthesia care unit (PACU) at once each on Post-operative day 1,2, and 3. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03250507
Study type Interventional
Source Henry Ford Health System
Contact
Status Completed
Phase Phase 4
Start date March 13, 2017
Completion date January 30, 2019
View Details
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